𝔖 Bobbio Scriptorium
✦   LIBER   ✦

cis,cis-Ceratospong­amide monohydrate

✍ Scribed by Doi, Mitsunobu ;Asano, Akiko

Publisher
International Union of Crystallography
Year
2002
Tongue
English
Weight
422 KB
Volume
58
Category
Article
ISSN
1600-5368

No coin nor oath required. For personal study only.

✦ Synopsis

Single-crystal X-ray study T = 100 K Mean '(C±C) = 0.006 A Ê R factor = 0.056 wR factor = 0.141 Data-to-parameter ratio = 16.4

For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.

📜 SIMILAR VOLUMES

The cis,cis-proline isomer of ceratospon
The cis,cis-proline isomer of ceratospong­amide
✍ Doi, Mitsunobu ;Yumiba, Aiko ;Asano, Akiko 📂 Article 📅 2001 🏛 International Union of Crystallography 🌐 English ⚖ 343 KB

## Ceratospongamide, cyclo(-Ile-Oxz-Phe-Pro-Thz-Phe-Pro-) (Oxz = oxazoline and Thz = thiazole), C 41 H 49 N 7 O 6 S, is a thiazole-containing cyclic peptide isolated from marine sources. Two stable isomers are known and the structure of the cis,cis-isomer has been determined. The peptide ring is f

ChemInform Abstract: Total Synthesis of
ChemInform Abstract: Total Synthesis of cis,cis-Ceratospongamide, a Bioactive Thiazole-Containing Cyclic Peptide from Marine Origin.
✍ Fumiaki Yokokawa; Hirofumi Sameshima; Takayuki Shioiri 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

cis,cis,cis,cis-1,3,5,7-Cyclononatetran
cis,cis,cis,cis-1,3,5,7-Cyclononatetran
✍ Dr. G. Boche; H. Böhme; D. Martens 📂 Article 📅 1969 🏛 John Wiley and Sons 🌐 English ⚖ 247 KB 👁 1 views

80 "C/0.003 Torr; UV-Spektrum (in n-Hexan): 302 (4.17), 270 (4.12), 260 (4.06) nm (log E ) ; NMR-Spektrum (in CDC13): Dublett zentriert bei 7 = 7.34 (4CH3). Multipletts zentriert bei T = 6.17 (H-3a, H-7a), bei 4.55 (H-2. H-3. H-4, H-5, H-6) und bei 3.65 (H-7)]. Das NMR-Spektrum von (5) erlaubt keine